Canonical Allele Identifier: PA101179
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 435060
ClinVar RCV Id: RCV000500817 RCV000633131 RCV001565138 RCV002367686 RCV004551628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Leu221Pro
CA374983528
NM_001114753.3:c.662T>C